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· · COA & SDS available for every product · Same-day shipping on in-stock items N-Acetyl-D-tryptophan - ≥98% , CAS No.2280-01-5
Synonyms
MLS001066362 | SMR000471873 | N-Acetyl-DL-Tryptophen | N-Acetyltryptophan # | 2-Acetylamino-3-(1H-indol-3-yl)-propionic acid | CHEBI:16734 | NCGC00096726-01 | (2R)-2-acetamido-3-(1H-indol-3-yl)propionic acid | C03137 | N-ACETYL-D-TRP-OH | DTXSID301018144
Storage
Store at 2-8°C,Argon charged
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
MLS001066362 | SMR000471873 | N-Acetyl-DL-Tryptophen | N-Acetyltryptophan # | 2-Acetylamino-3-(1H-indol-3-yl)-propionic acid | CHEBI:16734 | NCGC00096726-01 | (2R)-2-acetamido-3-(1H-indol-3-yl)propionic acid | C03137 | N-ACETYL-D-TRP-OH | DTXSID301018144
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Pubchem Sid 488189756 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488189756 Canonical Smiles CC(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)O IUPAC Name (2R)-2-acetamido-3-(1H-indol-3-yl)propanoic acid InChIKey DZTHIGRZJZPRDV-GFCCVEGCSA-N INCHI 1S/C13H14N2O3/c1-8(16)15-12(13(17)18)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7,12,14H,6H2,1H3,(H,15,16)(H,17,18)/t12-/m1/s1 Isomeric SMILES CC(=O)N[C@H](CC1=CNC2=CC=CC=C21)C(=O)O WGK Germany 3 Molecular Weight 246.26 Reaxy-Rn 487262 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=487262&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Class Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - N-acyl-alpha amino acids and derivatives Direct Parent N-acyl-alpha amino acids Alternative Parents Indolyl carboxylic acids and derivatives 3-alkylindoles Substituted pyrroles Benzenoids Heteroaromatic compounds Acetamides Secondary carboxylic acid amides Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents N-acyl-alpha-amino acid - Indolyl carboxylic acid derivative - 3-alkylindole - Indole - Indole or derivatives - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Monocarboxylic acid or derivatives - Carboxylic acid - Azacycle - Organoheterocyclic compound - Carbonyl group - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids. These are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. External Descriptors D-tryptophan derivative - N-acetyl-D-amino acid Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Insoluble in water, soluble in methanol, very slightly soluble in ether Sensitivity air sensitive ；light sensitive Melt Point(°C) 186°C Molecular Weight 246.260 g/mol XLogP3 1.100 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 4 Exact Mass 246.1 Da Monoisotopic Mass 246.1 Da Topological Polar Surface Area 82.200 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 332.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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